chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1177603210177603211GA39GENIChomozygous60969170
1177603640177603641GA29GENIChomozygous60969172
1177604146177604147TC30GENIChomozygous60969174
1177606006177606007CT30GENIChomozygous60969176
1177606686177606687CA38GENIChomozygous60969178
1177607561177607562AT25GENIChomozygous60969180
1177612088177612089AG35GENIChomozygous60969184
1177612817177612818CT29GENIChomozygous60969188
1177613540177613541CT33GENIChomozygous60969190
1177614914177614915CT37GENIChomozygous60969192
1177614961177614962TC35GENIChomozygous60969194
1177615613177615614TTGGG15GENIChomozygous61561617
1177615797177615798TC26GENIChomozygous60969198
1177616646177616647AG22GENIChomozygous60969200
1177616722177616723CA26GENIChomozygous60969202
1177616913177616914CT27GENIChomozygous60969204
1177617680177617681CT20GENIChomozygous60969206
1177619932177619933AG27GENIChomozygous60969208
1177621036177621037C-26GENIChomozygous60969210
1177621195177621196G-39GENIChomozygous60969212
1177621691177621692CT33GENIChomozygous60969214
1177622060177622061CT30GENIChomozygous60969216
1177622212177622213CT32GENIChomozygous60969218
1177624883177624884CT20GENIChomozygous60969220
1177625104177625105CT38GENIChomozygous60969222
1177626672177626673TG27GENIChomozygous60969224
1177627461177627462GA32GENICpossibly homozygous60969225
1177627588177627589CCTT11GENICpossibly homozygous60969227
1177627588177627589CCT11GENICheterozygous62178628
1177628609177628610TC26GENIChomozygous60969229
1177628849177628853ACAC----20GENIChomozygous61561618
1177628952177628953TTG5GENICheterozygous61561619
1177631429177631430CT27GENIChomozygous60969233
1177632309177632310GA28GENIChomozygous60969235
1177632546177632558ACACACACACAT------------7GENICpossibly homozygous60969237
1177634280177634281TA30GENIChomozygous61561621
1177634420177634421GA18GENIChomozygous60969239
1177634489177634491CC--7GENIChomozygous60969241